Abstract

BackgroundModeling of the immune system – a highly non-linear and complex system – requires practical and efficient data analytic approaches. The immune system is composed of heterogeneous cell populations and hundreds of cell types, such as neutrophils, eosinophils, macrophages, dendritic cells, T cells, and B cells. Each cell type is highly diverse and can be further differentiated into subsets with unique and overlapping functions. For example, CD4+ T cells can be differentiated into Th1, Th2, Th17, Th9, Th22, Treg, Tfh, as well as Tr1. Each subset plays different roles in the immune system. To study molecular mechanisms of cell differentiation, computational systems biology approaches can be used to represent these processes; however, the latter often requires building complex intracellular signaling models with a large number of equations to accurately represent intracellular pathways and biochemical reactions. Furthermore, studying the immune system entails integration of complex processes which occur at different time and space scales.MethodsThis study presents and compares four supervised learning methods for modeling CD4+ T cell differentiation: Artificial Neural Networks (ANN), Random Forest (RF), Support Vector Machines (SVM), and Linear Regression (LR). Application of supervised learning methods could reduce the complexity of Ordinary Differential Equations (ODEs)-based intracellular models by only focusing on the input and output cytokine concentrations. In addition, this modeling framework can be efficiently integrated into multiscale models.ResultsOur results demonstrate that ANN and RF outperform the other two methods. Furthermore, ANN and RF have comparable performance when applied to in silico data with and without added noise. The trained models were also able to reproduce dynamic behavior when applied to experimental data; in four out of five cases, model predictions based on ANN and RF correctly predicted the outcome of the system. Finally, the running time of different methods was compared, which confirms that ANN is considerably faster than RF.ConclusionsUsing machine learning as opposed to ODE-based method reduces the computational complexity of the system and allows one to gain a deeper understanding of the complex interplay between the different related entities.

Highlights

  • Modeling of the immune system – a highly non-linear and complex system – requires practical and efficient data analytic approaches

  • We have developed Enteric Immunity Simulator (ENISI) MSM, a multiscale modeling platform driven by high-performance computing and designed for computational immunology, which integrates agent based modeling (ABM), Ordinary differential equation (ODE) and partial differential equations (PDEs) [48]

  • The lm function is used to fit linear models, which can be used to carry out regression, single stratum analysis of variance and analysis of covariance [61]

Read more

Summary

Introduction

Modeling of the immune system – a highly non-linear and complex system – requires practical and efficient data analytic approaches. To study molecular mechanisms of cell differentiation, computational systems biology approaches can be used to represent these processes; the latter often requires building complex intracellular signaling models with a large number of equations to accurately represent intracellular pathways and biochemical reactions. Immune cell differentiation and modeling The process of immune cell differentiation plays a central role in orchestrating immune responses This process is based on the differentiation of naïve immune cells that, upon activation of their transcriptional machinery through a variety of signaling cascades, become phenotypically and functionally different entities capable of responding to a wide range of viruses, bacteria, parasites, or cancer cells. SBML allows the encoding of biological process including their dynamics This information can be unambiguously converted into a system of Ordinary Differential Equations (ODEs). Several equations are usually required to adequately represent these complex immunological processes, being either at the level of the whole organism, tissue, cells or molecules

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call